A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2683n100



Internal ID20154299
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:101684138..101808429hg38UCSC Ensembl
chr15:102224341..102348632hg19UCSC Ensembl
chr15:100041864..100166155hg18UCSC Ensembl
Cytoband15q26.3
Allele length
AssemblyAllele length
hg38124292
hg19124292
hg18124292
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1043517, nsv1038859
Samples
Known GenesOR4F6, TARSL2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv2683n100
Frequency
Sample Size29084
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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